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Structure of 91103-37-6
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tert-Butyl (S)-(1-hydroxybut-3-en-2-yl)carbamate, 97% (stabilized with MEHQ) features a chiral allylic alcohol moiety with high stereochemical integrity. This bench-stable, moisture-tolerant reagent integrates seamlessly into asymmetric synthesis workflows, enabling efficient access to functionalized intermediates via selective transformations.
tert-Butyl (S)-(1-hydroxybut-3-en-2-yl)carbamate, 97% (stabilized with MEHQ) serves as a chiral building block for stereoselective synthesis, enabling efficient access to (S)-configured intermediates via allylic functionalization. The protected hydroxyl group exhibits excellent bench stability and compatibility with standard coupling reactions, while the enol ether functionality facilitates selective transformations under mild conditions. Its robustness in purification and broad functional group tolerance make it a practical choice for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: